Essential Functions
- Provide clinical research support to investigators and site staff, including
- Verify and/or correct research study information on source documents; research queries and variances; and provide
feedback to the site data collector.
- Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control for content,
accuracy, and completeness.
- Prepare and maintain research study files.
Compile, collate and submit study information within established deadlines.
- Collect and submit regulatory/ethics documentation pertaining to the research study.
- Maintain the FDA 1572 form for assigned research studies.
- Input visit data into clinical trial management system (CTMS) to track patient visits and procedures completed against the study budget.
**Qualifications**:
- High School Diploma or equivalent High School Diploma Req
- Educational equivalent and 2 years' relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience Req
- Basic knowledge of clinical trials
- In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study
schedules
- Basic knowledge of medical terminology
- Excellent interpersonal skills
- Ability to pay close attention to detail
- Ability to establish and maintain effective working relationships with coworkers, managers and clients
- Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies Upon Hire Req
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world.
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